Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders.

MENTAL illness genetics; MENTAL illness risk factors; ATTENTION-deficit hyperactivity disorder; AUTISM; BRAIN; CEREBELLUM; MENTAL depression; GENE expression; GENOMES; BIPOLAR disorder; MENTAL illness; SCHIZOPHRENIA; GENE expression profiling; DESCRIPTIVE statistics

Background: Mounting evidence shows genetic overlap between multiple psychiatric disorders. However, the biological underpinnings of shared risk for psychiatric disorders are not yet fully uncovered. The identification of underlying biological mechanisms is crucial for the progress in the treatment of these disorders. Methods: We applied gene-set analysis including 7372 gene sets, and 53 tissue-type specific gene-expression profiles to identify sets of genes that are involved in the etiology of multiple psychiatric disorders. We included genome-wide meta-association data of the five psychiatric disorders schizophrenia, bipolar disorder, major depressive disorder, autism spectrum disorder, and attention-deficit/hyperactivity disorder. The total dataset contained 159 219 cases and 262 481 controls. Results: We identified 19 gene sets that were significantly associated with the five psychiatric disorders combined, of which we excluded five sets because their associations were likely driven by schizophrenia only. Conditional analyses showed independent effects of several gene sets that in particular relate to the synapse. In addition, we found independent effects of gene expression levels in the cerebellum and frontal cortex. Conclusions: We obtained novel evidence for shared biological mechanisms that act across psychiatric disorders and we showed that several gene sets that have been related to individual disorders play a role in a broader range of psychiatric disorders. [ABSTRACT FROM AUTHOR]

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